Aesthetic and Reconstructive Technologies, Inc.

FDA Regulatory Profile

Aesthetic and Reconstructive Technologies, Inc. appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 23, 2003.

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023678DIMISIL SCAR GELJanuary 23, 2003
K022306AART SILICONE TUBINGOctober 10, 2002
K022511AART CALF IMPLANTAugust 26, 2002
K022223AART SILICONE SHEETINGAugust 8, 2002
K021820AART SILICONE CARVING BLOCKJuly 16, 2002
K021839AART GLUTEAL IMPLANTJuly 16, 2002
K021337AART PECTORALIS IMPLANTJuly 3, 2002
K021419AART MALAR IMPLANTJuly 2, 2002
K021417AART CHIN IMPLANTJuly 2, 2002
K021418AART NASAL IMPLANTJuly 2, 2002